In early 2021, the U.S. Food and Drug Administration (FDA) issued a safety communication for Stryker STAR Ankle implants. The statement advised patients, caregivers, and health care providers about the dangers, risks, and failures of the product. An FDA study found that use of the device is connected to a higher-than-expected risk of fracturing in the polyethylene component.
Fracturing may lead to:
- Ankle and/or bodily pain
- Joint instability
- Revision surgery
- Loss of mobility
What is the issue with the STAR ankle device?
The Stryker Scandinavian Total Ankle Replacement (STAR) device is used to replace failed/failing ankle joints that have been impacted and damaged by symptoms such as osteoarthritis, post-traumatic arthritis, or rheumatoid arthritis.
Patients with any of the aforementioned conditions (osteoarthritis, post-traumatic arthritis, or rheumatoid arthritis), who lead an active lifestyle, or patients under 55 years old face an elevated risk of fracture of the STAR Ankle implant.
Alex Davis Law is ready to help
If you have suffered any of these complications from a Stryker STAR implant, you may be entitled to financial compensation. To review your case, contact the lawyers at Alex Davis Law to schedule a free consultation today.
